Canonical Allele Identifier: CA334723705
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs985319743
gnomAD v2: X-115304818-A-C
gnomAD v3: X-116173565-A-C
gnomAD v4: X-116173565-A-C
MyVariant Identifiers: chrX:g.115304818A>C (hg19) chrX:g.116173565A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173565A>C , CM000685.2:g.116173565A>C GRCh38
NC_000023.10:g.115304818A>C , CM000685.1:g.115304818A>C GRCh37
NC_000023.9:g.115218846A>C NCBI36
NG_016326.1:g.7861A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*193A>C MANE Select ENSP00000360973.4:n.*193A>C
ENST00000371906.4:c.*193A>C ENSP00000360973.4:n.*193A>C
NM_000686.4:c.*193A>C NP_000677.2:n.*193A>C
XM_011537533.1:c.*193A>C XP_011535835.1:n.*193A>C
NM_000686.5:c.*193A>C MANE Select NP_000677.2:n.*193A>C
NM_001385624.1:c.*193A>C NP_001372553.1:n.*193A>C
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